Newsletter | October 28, 2024

10.28.24 -- Tune Therapeutics On Clinical Readiness, Technology Adoption

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It's no secret that on-going research aims to improve the efficacy and specificity of non-viral approaches for genetic engineering. But the field is rapidly evolving with research aimed at improving transfection efficiency, targeting, and safety profiles of non-viral delivery systems. Join Cell & Gene Live to discuss the most notable approaches and recent breakthroughs as well as promising non-viral vectors used in clinical trials. Attendance is free thanks to the support of MaxCyte.

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Tune Therapeutics On Clinical Readiness, Technology Adoption

Heidi Zhang, Ph.D., explains Tune Therapeutics' epigenetic approach to gene therapy and how the company is preparing its lead candidate for the clinic, as well as it's modular approach to automation.

The Role Of Allogeneic Treatments In The Future Of Cell Therapy

Review considerations for a successful development and manufacturing process and learn how finding an experienced partner can help you overcome hurdles on the path to IND.

Analytical Testing: Sequencing Methods For Nucleic Acids, Therapeutics

Leveraging an experienced partner's expertise in GMP-grade plasmid manufacturing and advanced analytical methods can accelerate the development and success of your next-generation therapies.

Response To FDA Black Box Warning

The FDA has launched an investigation into the risk of T-cell malignancies following CAR-T cell immunotherapies. Review the key points of this announcement concerning the CGT research community.

Set Your Cell And Gene Therapy Program Up For Success From Day One

Partner with a specialized CDMO early in your CGT development to ensure a streamlined path from discovery to successful commercialization, avoiding costly pitfalls and delays.

The Future Of Plasmid DNA Upstream Optimization

An optimized upstream manufacturing process is crucial for producing the necessary amount of plasmid DNA required for the growing number of therapeutic and vaccine applications available.

Exploring The Cost Considerations Of Immune Cell Therapies

Immune cell therapies have incredible potential for cancer treatment, and making them more cost effective is a critical consideration for improving patient access and outcomes.

How To Apply Quality By Design Principles To CGT Release Testing

In this presentation, speakers discuss how to develop and use QC assays that can facilitate both product and process understanding and control.

New Perspectives On Accelerating Genetic Nanomedicines

Discover how regulatory bodies are adopting a risk-based approach to address the unique challenges of genetic nanomedicines, and stakeholder engagement is essential.

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Developers often aim to cut expenses during development. Discover the long-term outcomes of cost-effective measures like using RUO leukopaks compared to investing in high-quality GMP-grade vectors.

OUTSOURCING SOLUTIONS

Accelerating The Delivery Of Innovative Cell Therapies - BioCentriq

RNA, Cell, Protein, And Vector Engineering - ElevateBio

mRNA-LNP CDMO Services - Vernal Biosciences

AAV Biosafety Testing And Characterization Services - MilliporeSigma

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